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Progesterone Determination Kit - India CDSCO Medical Device Registration

Progesterone Determination Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000246_e008f6314ecec87d1f86965a0b610969_6a296a8ebe695cd9bb56220746157831. This device is marketed under the brand name hba1c. The license holder is Allied Biotechnology India Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class B
Progesterone Determination Kit
UID: IMP/IVD/2022/000246_e008f6314ecec87d1f86965a0b610969_6a296a8ebe695cd9bb56220746157831

Brand Name

hba1c

Device Class

Class B

Approving Authority

CDSCO

Product Information

The reagents are used for quantitative determination of progesterone in human serum, plasma and whole blood in vitro. They areย for professional use only

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